A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6345586



Internal ID21003139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:135794095..135807996hg38UCSC Ensembl
chr2:136551665..136565566hg19UCSC Ensembl
Cytoband2q21.3
Allele length
AssemblyAllele length
hg3813902
hg1913902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206585
Samples
Known GenesLCT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6345586
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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